Abstract
Here, we report accessing small 3-fluoropyrrolidines and 3,3-difluoropyrrolidines through a 1,3-dipolar cycloaddition with a simple azomethine ylide and a variety of vinyl fluorides and vinyl difluorides. We demonstrate that vinyl fluorides within α,β-unsaturated, styrenyl and even enol ether systems can participate in the cycloaddition reaction. The vinyl fluorides are relatively easy to synthesize through a variety of methods, making the 3-fluoropyrrolidines very accessible.
Cite
CITATION STYLE
McAlpine, I., Tran-Dubé, M., Wang, F., Scales, S., Matthews, J., Collins, M. R., … O’Neill, B. T. (2015). Synthesis of Small 3-Fluoro- and 3,3-Difluoropyrrolidines Using Azomethine Ylide Chemistry. Journal of Organic Chemistry, 80(14), 7266–7274. https://doi.org/10.1021/acs.joc.5b00853
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.